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CCLONES - ADEPT ( Comparing Clonal Lines On Experimental Sites)

CCLONES - ADEPT ( Comparing Clonal Lines On Experimental Sites). Forest Biology Research Cooperative University of Florida. ‘Series 1’ CCLONES Schedule. Breeding 1996-1997 Sow seed March 2000 Top seedlings June 2000 Transplant seedling hedges Sept 2000

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CCLONES - ADEPT ( Comparing Clonal Lines On Experimental Sites)

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  1. CCLONES - ADEPT(Comparing Clonal Lines On Experimental Sites) Forest Biology Research Cooperative University of Florida

  2. ‘Series 1’ CCLONES Schedule • Breeding 1996-1997 • Sow seed March 2000 • Top seedlings June 2000 • Transplant seedling hedges Sept 2000 • Randomize hedges on pad April 2001 • Stick cuttings for rooting assessment1 May 2001 • Stick cuttings for rooting assessment2 July 2001 • Stick cuttings for Study B field tests Jan & May 2002 • Screen 1400 clones for rust and PC 2002 • Plant 915 clones on six locations December 2002 • Measure phenotypes 2003

  3. Breeding • 30 top loblolly parents • Half from coastal plain; half from Florida • “Good” for growth and rust, but variation among parents • 70 full-sib families • Partial diallel with approx 4 to 5 crosses per parent • Intent is to go to the field with 60 FS fams

  4. 32 elite parents crossed in partial diallel to create ~2200 clones from 70 full-sib families Seed stratified: 1/24/00 Seed sown: 3/3/00

  5. Study B seedlings after hedging (left) and prior to hedging (right) Seedlings were hedged in June 2000.

  6. Hedged FBRC Study B seedlings 6 weeks after hedging.

  7. Close-up of individual hedge six weeks after hedging.

  8. Close-up of individual hedge twelve weeks after hedging.

  9. Hedges moved to 20,000 sq ft hedge-pad after transplanting

  10. Experimental Design • Randomization • Clonal hedges were completely randomized on the hedge pad prior to setting • Fixed-tray system (135 cells) • Trays could then be randomized within each rep

  11. Clonal hedges were randomized in April 2001.

  12. ‘Series 1’ CCLONES Schedule • Sow seed March 2000 • Top seedlings June 2000 • Transplant seedling hedges Sept 2000 • Randomize hedges on pad April 2001 • Stick cuttings for rooting assessment1 May 2001 • Stick cuttings for rooting assessment2 July 2001 • Stick cuttings for Study B field tests Jan & May 2002 • Screen 1400 clones for rust and PC 2002 • Plant 915 clones on six locations December 2002 • Measure phenotypes 2003

  13. May 7, 2001 -61 weeks after sowing -46 weeks after initial topping of seedling -11 weeks after last hedging

  14. July

  15. Shoot Collection

  16. Preparing Cuttings To Set

  17. 30 Clones Per Tray

  18. Typical Rooted Cutting(9 Weeks from setting)

  19. Root AssessmentExperimental Design • May 2001 setting • Set ~2200 clones, 4 replications with 4-ramet row plots • Assessed rooting 9 weeks after setting • Counted # newly emerging roots from plug 9 weeks after setting • Shoot dry weights obtained from 1 ramet per clone per rep (3 reps) • Variance components estimated with ASREML • July 2001 setting • Set ~2200 clones, 5 replications with 4-ramet row plots • Assessed rooting 9 weeks after setting • Measured cutting diameter and height 9 weeks after setting (3 reps) • Variance components estimated with ASREML

  20. Summary of Rooting

  21. Variation Within Family for Rooting

  22. Heritability Estimates For Root Number and Rooting % D/A = 0.16 D/A = 0.05 D/A = 0.14

  23. Differences in Shoot Morphology Do these differences have an effect on rooting? 64% rooting 48% rooting 81% rooting

  24. Differences in Root Morphology

  25. ‘Series 1’ CCLONES Schedule • Breeding 1996-1997 • Sow seed March 2000 • Top seedlings June 2000 • Transplant seedling hedges Sept 2000 • Randomize hedges on pad April 2001 • Stick cuttings for rooting assessment1 May 2001 • Stick cuttings for rooting assessment2 July 2001 • Stick cuttings for Study B field tests Jan & May 2002 • Screen 1400 clones for rust and PC 2002 • Plant 915 clones on six locations December 2002 • Measure phenotypes 2003

  26. Disease Screening • 1400 clones from May and July setting sent to RSC • 22,000 rooted cuttings • 5 to 20 ramets per clones • Good rooting clones with approx equal numbers per family • Four groups (with 5 or less ramets per clones) • Group 1: Rust with broad inoculum • Group 2: Rust with narrow inoculum • Group 3: PC with broad inoculum • Group 4: PC with narrow inoculum • Measure phenotypes (disease symptoms): • 1400 clones • Two very different pathosytems

  27. Resistance Screening at USFS - RSC

  28. ‘Series 1’ CCLONES Schedule • Breeding 1996-1997 • Sow seed March 2000 • Top seedlings June 2000 • Transplant seedling hedges Sept 2000 • Randomize hedges on pad April 2001 • Stick cuttings for rooting assessment1 May 2001 • Stick cuttings for rooting assessment2 July 2001 • Stick cuttings for Study B field tests Jan & May 2002 • Screen 1400 clones for rust and PC 2002 • Plant 915 clones on six locations December 2002 • Measure phenotypes 2003

  29. Field Locations • Six Locations in FL and GA • Design at each location: • 2 silvicultural treatments (HI and LO) • 4 complete blocks per treatment • Total of 8 ramets per clone (2 x 4) per site • 915 clones from 60 FS families • Total size approx 14 acres • Total trees: 6 sites x 2 trts x 4 blocks x 915 clones = 44,000 • Two settings: Jan and April • Jan setting used for 3 sites • April setting used for three sites • Field planting in Dec 2002

  30. Phenotyping of Association Pop’n • Rooting • May and July 2001 • Jan and April 2002 • Disease symptoms • Rust and PC in RSC • Rust in HI and LO treatments in field • Standard growth:1, 2, 3 height in HI and LO • Water deficit symptoms: 2 of 6 sites; 600 clones • Stable carbon isotopes at end of 1st season • Specific leaf area • Relative water content – two dry periods • Water potential – two dry periods • Other????

  31. Acknowledgements Forest Biology Research Cooperative Special thanks to International Paper

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